ClinVar Miner

List of variants in gene MTAP reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_002451.4(MTAP):c.*1453C>T rs753610558 0.00096
NM_002451.4(MTAP):c.*3072G>A rs768885564 0.00083
NM_002451.4(MTAP):c.*3052C>T rs182636316 0.00053
NM_002451.4(MTAP):c.*2651G>A rs569725867 0.00044
NM_002451.4(MTAP):c.*2968T>C rs554780978 0.00022
NM_002451.4(MTAP):c.*1482A>G rs560361151 0.00020
NM_002451.4(MTAP):c.*3361C>T rs138870323 0.00018
NM_002451.4(MTAP):c.*2033G>A rs547939395 0.00017
NM_002451.4(MTAP):c.*2481T>C rs937544830 0.00017
NM_002451.4(MTAP):c.*2837T>A rs566068002 0.00014
NM_002451.4(MTAP):c.*1384G>C rs755911467 0.00013
NM_002451.4(MTAP):c.*2912G>C rs775831366 0.00013
NM_002451.4(MTAP):c.*2269A>T rs760747427 0.00012
NM_002451.4(MTAP):c.*102A>G rs755040797 0.00010
NM_002451.4(MTAP):c.*2638G>A rs556394357 0.00009
NM_002451.4(MTAP):c.*2660C>A rs78176424 0.00009
NM_002451.4(MTAP):c.*3389T>C rs765432220 0.00008
NM_002451.4(MTAP):c.*1760A>G rs886063788 0.00007
NM_002451.4(MTAP):c.*3057T>A rs887122969 0.00007
NM_002451.4(MTAP):c.-52G>C rs949068748 0.00007
NM_002451.4(MTAP):c.224A>G (p.Gln75Arg) rs764365358 0.00007
NM_002451.4(MTAP):c.*2937C>G rs536527668 0.00005
NM_002451.4(MTAP):c.*3060A>G rs1179074073 0.00005
NM_002451.4(MTAP):c.*3206C>T rs886063793 0.00005
NM_002451.4(MTAP):c.*395A>G rs1050551130 0.00005
NM_002451.4(MTAP):c.*3276A>G rs1038408600 0.00004
NM_002451.4(MTAP):c.*3774A>G rs949366316 0.00004
NM_002451.4(MTAP):c.*2383C>T rs886063791 0.00003
NM_002451.4(MTAP):c.*3160T>C rs1228548595 0.00003
NM_002451.4(MTAP):c.*3501T>C rs949232383 0.00003
NM_002451.4(MTAP):c.300G>A (p.Glu100=) rs762121645 0.00003
NM_002451.4(MTAP):c.*1093G>T rs1825785660 0.00001
NM_002451.4(MTAP):c.*1399C>A rs1825792275 0.00001
NM_002451.4(MTAP):c.*2183T>C rs1825811023 0.00001
NM_002451.4(MTAP):c.*2286A>G rs1825813138 0.00001
NM_002451.4(MTAP):c.*2606G>C rs886063792 0.00001
NM_002451.4(MTAP):c.*3766C>T rs149649469 0.00001
NM_002451.4(MTAP):c.*730A>G rs1031531828 0.00001
NM_002451.4(MTAP):c.*912A>G rs1825783181 0.00001
NM_002451.4(MTAP):c.-108_-103del rs886063780 0.00001
NM_002451.4(MTAP):c.*1140A>G rs886063785
NM_002451.4(MTAP):c.*1197C>G rs886063786
NM_002451.4(MTAP):c.*1558G>C rs989103885
NM_002451.4(MTAP):c.*1608del rs886063787
NM_002451.4(MTAP):c.*1621_*1622del rs11358276
NM_002451.4(MTAP):c.*1668T>C rs1040775189
NM_002451.4(MTAP):c.*1831T>A rs886063789
NM_002451.4(MTAP):c.*1836C>G rs768066844
NM_002451.4(MTAP):c.*2111A>G rs1825809798
NM_002451.4(MTAP):c.*2171G>A rs886063790
NM_002451.4(MTAP):c.*2333C>G rs1587259830
NM_002451.4(MTAP):c.*254A>T rs897835622
NM_002451.4(MTAP):c.*258del rs886063782
NM_002451.4(MTAP):c.*2693G>A rs1825822182
NM_002451.4(MTAP):c.*2740G>A rs1460775302
NM_002451.4(MTAP):c.*303G>A rs140440868
NM_002451.4(MTAP):c.*3656A>G rs1825841895
NM_002451.4(MTAP):c.*3692G>A rs1418873617
NM_002451.4(MTAP):c.*378T>C rs886063783
NM_002451.4(MTAP):c.*3943G>A rs886063794
NM_002451.4(MTAP):c.*795A>T rs1317482370
NM_002451.4(MTAP):c.119A>G (p.Lys40Arg) rs760959805
NM_002451.4(MTAP):c.187A>G (p.Arg63Gly) rs886063781

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